| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7931869-7932253 | Common:5; Rare:101 | ||||
| chr17:8151174-8151498 | Common:3; Rare:81 | ||||
| chr17:8152352-8152719 | Common:4; Rare:89 | ||||
| chr17:8156821-8156869 | Common:2; Rare:20 | ||||
| chr17:8248050-8248166 | Common:3; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:8435705-8436034 | Common:4; Rare:125 | ||||
| chr17:8630652-8630790 | Rare:44 | ||||
| chr17:10697460-10697661 | Common:4; Rare:92; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:10730014-10730129 | Common:1; Rare:25 | ||||
| chr17:14069368-14069580 | Common:2; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:14300773-14301116 | Common:3; Rare:90 | ||||
| chr17:15260787-15260898 | Rare:46 | ||||
| chr17:15699500-15699797 | Common:3; Rare:79 | ||||
| chr17:15999579-16000028 | Common:3; Rare:188; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217058-16217228 | Rare:37 |